If a base is merely substituted, the reading frame remains altered only by that one base, which may or may not change the amino acid encoded in the codon. If a base were inserted or deleted, there will be a reading frame shift which would have a profound effect on the amino acids encoded.
For example, a sample of RNA has the following sequence:
AUG AUA AAG CUA CCG GGC UAG ...
which translates to M-I-K-L-P-G
If the second condon changed from AUA to AUC, then the amino acid sequence would remain the same.
If the second condon were to have its second A deleted, then the entire amino acid sequence changes to:
M-I-S-T-R-A...
A frameshift mutation, such as an insertion or deletion of a nucleotide, that occurs just after the AUG start codon is likely to have the most serious effect on the polypeptide product. This is because frameshift mutations shift the reading frame of the mRNA sequence, causing all subsequent codons to be read incorrectly, leading to a completely altered polypeptide sequence.
If a chromosome lacks certain genes, it is likely due to a genetic mutation or deletion event that occurred during DNA replication or recombination. This can lead to genetic disorders or abnormalities depending on the specific genes that are missing.
A deletion of one nitrogen base would result in a frameshift mutation in the DNA sequence that codes for proteins. This would likely affect all amino acids downstream of the deletion site, leading to a significant alteration in the protein's primary sequence and possibly its function.
A single-nucleotide substitution causing a missense mutation that changes a critical amino acid in the protein's active site or functional domain is most likely to have a catastrophic effect on the protein's function. This type of mutation can disrupt the protein's structure or its ability to interact with other molecules, leading to severe functional impairment.
A compound that is structurally and functionally similar to the hormone would be most likely to mimic its effects on sexual behavior. These compounds are called agonists and can bind to the hormone's receptor and trigger a similar response in the body.
A frameshift mutation, such as an insertion or deletion of a nucleotide, that occurs just after the AUG start codon is likely to have the most serious effect on the polypeptide product. This is because frameshift mutations shift the reading frame of the mRNA sequence, causing all subsequent codons to be read incorrectly, leading to a completely altered polypeptide sequence.
A single change in the primary sequence of bases can result in complete misfolding of proteins. The most likely serious change would be addition or deletion of a base, a substitution would be less likey to be as serious but can also render a protein inactive.
The three types of anomalies likely to show up are: Insertion, Deletion, and Update anomalies.
If a chromosome lacks certain genes, it is likely due to a genetic mutation or deletion event that occurred during DNA replication or recombination. This can lead to genetic disorders or abnormalities depending on the specific genes that are missing.
The minimum dosage to be effective is 50mg, three times a day, morning around 8 am, 2pm and 9pm are the optimal times You would likely notice side effects within a week, but serious side effects are rare
The MOST serious effect would be death.
A deletion of one nitrogen base would result in a frameshift mutation in the DNA sequence that codes for proteins. This would likely affect all amino acids downstream of the deletion site, leading to a significant alteration in the protein's primary sequence and possibly its function.
People with liver disease may be more likely to have side effects from ondansetron.
D
The likely word is the adjective serious (severe, or not humorous)
She will likely enjoy it but just as likely remain a virgin
Yes, but it would be very - very - VERY rare. Chlamydia does serious damage quick, so having it for "years" without having severe side effects is really not likely.